H. Abouzeid

Discipline

Psychologie (1)

Type de document

Articles (6)

Co-auteur

Date

Source

Mot-clé

gène (5) Patients (5) Human beings (5) Patients (5) Cases (4) Eye (4) Cases (4) mutation (3) Development (3) Methods (3) Phenotype (3) Families (3) Example (3) Methods (3) Mutation (3) roman (3) association (2) modèle (2) perte (2) famille (2) ADN (2) maladie (2) Causative (2) Case (2) Genes (2) Origin (2) Social groups (2) Sex (2) Retinal (Visual pigment) (2) Retina (2)

Documents écrit par H. Abouzeid (6) | parle de H. Abouzeid (0)

Genome-wide Association Studies of Retinal Vessel Tortuosity Identify Numerous Novel Loci Revealing Genes and Pathways Associated With Ocular and Cardiometabolic Diseases.
N. Mounier et al.
Intraocular Pressure Reduction after Femtolaser Assisted Cataract Surgery and Its Association with the Use of Ultrasound.
H. Abouzeid et al. (1 mai 2021)
ALDH1A3 loss of function causes bilateral anophthalmia/microphthalmia and hypoplasia of the optic nerve and optic chiasm.
M. Yahyavi et al. (2013)
VAX1 mutation associated with microphthalmia, corpus callosum agenesis and orofacial clefting-the first description of a VAX1 phenotype in humans.
A.M. Slavotinek et al. (2012)
RAX and anophthalmia in humans: Evidence of brain anomalies.
H. Abouzeid et al. (2012)
Germline mutations in retinoma patients: relevance to low-penetrance and low-expressivity molecular basis.
H. Abouzeid et al. (2009)